4 results for author:"Boumil R.M." in Literature citations
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| A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice. Boumil R.M., Letts V.A., Roberts M.C., Lenz C., Mahaffey C.L., Zhang Z.W., Moser T., Frankel W.N. PLoS Genet. 6:0-0(2010) · Mapped (8) |
| Absence seizures in C3H/HeJ and knockout mice caused by mutation of the AMPA receptor subunit Gria4. Beyer B., Deleuze C., Letts V.A., Mahaffey C.L., Boumil R.M., Lew T.A., Huguenard J.R., Frankel W.N. Hum. Mol. Genet. 17:1738-1749(2008) · Mapped (19) |
| The roles of MAD1, MAD2 and MAD3 in meiotic progression and the segregation of nonexchange chromosomes. Cheslock P.S., Kemp B.J., Boumil R.M., Dawson D.S. Nat. Genet. 37:756-760(2005) · Mapped (3) |
| A role for centromere pairing in meiotic chromosome segregation. Kemp B., Boumil R.M., Stewart M.N., Dawson D.S. Genes Dev. 18:1946-1951(2004) · Mapped (2) |